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rs1057521741

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521741(C;G)
Make rs1057521741(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position41332245
GeneTGFB1
is asnp
is mentioned by
dbSNPrs1057521741
dbSNP (old)rs1057521741
ClinGenrs1057521741
ebirs1057521741
HLIrs1057521741
Exacrs1057521741
Gnomadrs1057521741
Varsomers1057521741
LitVarrs1057521741
Maprs1057521741
PheGenIrs1057521741
Biobankrs1057521741
1000 genomesrs1057521741
hgdprs1057521741
ensemblrs1057521741
gopubmedrs1057521741
geneviewrs1057521741
scholarrs1057521741
googlers1057521741
pharmgkbrs1057521741
gwascentralrs1057521741
openSNPrs1057521741
23andMers1057521741
23andMe allrs1057521741
SNPshotrs1057521741
SNPdbers1057521741
MSV3drs1057521741
GWAS Ctlgrs1057521741
Max Magnitude0
ClinVar
Risk rs1057521741(G;G)
Alt rs1057521741(G;G)
Reference Rs1057521741(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFB1
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.41838150G>C
CLNSRC
CLNACC RCV000445099.1,